Canonical Allele Identifier: CA1763924478
Gene: BLK HGNC NCBI

Linked Data

dbSNP Id: rs1225405874

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491407T>A , CM000670.2:g.11491407T>A GRCh38
NC_000008.10:g.11348916T>A , CM000670.1:g.11348916T>A GRCh37
NC_000008.9:g.11386325T>A NCBI36
NG_023543.1:g.2396T>A
NG_023543.2:g.2396T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.274+4240T>A
ENST00000696154.1:c.-91+4240T>A ENSP00000512445.1:n.-91+4240T>A
ENST00000645242.1:c.-91+4240T>A ENSP00000494690.1:n.-91+4240T>A